催化铁与生物法耦合除磷工艺特性简

为了研究催化铁与生物耦合后对生物除磷特性的影响，实验采用人工配水用厌氧/好氧间歇流式富集培养聚磷微生物。对比发现，催化铁与生物耦合组中厌氧末段ORP降低了约60 mV，pH值小幅度的上升（≤0.3），整个培养过程中铁离子的浓度开始快速增加，之后趋于稳定（约40 mg Fe/g MLSS）。对好氧末段污泥SVI值比较发现，耦合工艺污泥沉降性能得到改善。除磷曲线比较发现，耦合组中厌氧末段磷的释放量下降，而好氧阶段磷的吸收速率增加；胞内聚合物提取表明，耦合组厌氧末段聚磷菌细胞内PHA含量有提高，好氧末段糖原含量有下降。磷形态提取分析表明，耦合组好氧末段污泥中无机态PO^3-₄-P含量更高。低浓度铁离子可以起到与生物耦合同步除磷的目的，本工艺长期运行未发现耦合体系中催化铁对除磷的抑制作用。     

催化铁与生物法耦合除磷工艺特性

为了研究催化铁与生物耦合后对生物除磷特性的影响，实验采用人工配水用厌氧／好氧间歇流式富集培养聚磷微生物。对比发现，催化铁与生物耦合组中厌氧末段ORP降低了约60mV，pH值小幅度的上升（≤0．3），整个培养过程中铁离子的浓度开始快速增加，之后趋于稳定（约40mgFe／gMLSS）。对好氧末段污泥SVI值比较发现，耦合工艺污泥沉降性能得到改善。除磷曲线比较发现，耦合组中厌氧末段磷的释放量下降，而好氧阶段磷的吸收速率增加；胞内聚合物提取表明，耦合组厌氧末段聚磷菌细胞内PHA含量有提高，好氧末段糖原含量有下降。磷形态提取分析表明，耦合组好氧末段污泥中无机态PO3 4-- P含量更高。低浓度铁离子可以起到与生物耦合同步除磷的目的，本工艺长期运行未发现耦合体系中催化铁对除磷的抑制作用。     

铁盐化学除磷对活性污泥生物除磷系统的影响

在小型处理系统中生物除磷同步化学除磷简便易行,但加入的除磷剂本身和形成的化学沉淀物的积累可能会对生物系统造成影响。采用序批式生物反应器,对铁盐的2种投加剂量下对活性污泥系统的影响进行了研究。结果表明,向SBR系统中连续投加15 mg·L~(-1)三氯化铁,表观上系统总体的除磷效率较未投加前有一定幅度的提高,活性污泥的沉降性能得到改善,但这削弱了系统的内在生物除磷效力。随着化学除磷的进行,系统污泥胞内PHA含量减少、糖原含量增加;污泥中PAOs相对数量下降而GAOs的相对数量显著增加,优势菌发生演替。结束投加后,污泥的活性可以缓慢恢复。说明该浓度下长时间连续进行同步化学与生物除磷,会对系统造成一定的损害,但这种损害在停止化学除磷后具有一定的可恢复性。而连续投加3 mg·L~(-1)三氯化铁的SBR系统总体除磷效率较未投加前有所提高,且没有对生物除磷系统产生明显抑制作用,能够较好实现化学除磷和生物除磷的协同。     

长期缺氧吸磷驯化下强化生物除磷系统污泥除磷方式的转化

采用交替厌氧/缺氧/好氧运行的序批式活性污泥反应器(SBR),通过梯度投加电子受体NO_3~-,考察长期缺氧吸磷驯化下强化生物除磷(EBPR)系统的性能及除磷方式的转化。结果表明,当进水COD为300～450mg/L、PO_4~(3-)(以P计,下同)和氨氮分别为8、14mg/L时,驯化期间TN去除率均保持在75%以上,长期缺氧吸磷驯化对COD和氨氮的去除没有影响。硝态氮投加量为5mg/L时,EBPR系统因电子受体投加不足除磷性能迅速恶化,增加硝态氮投加量至10mg/L,经过近30d的恢复,缺氧吸磷率最高可达97.67%,进一步提高硝态氮投加量至15mg/L,系统内硝态氮的积累导致缺氧吸磷率下降。污泥吸磷小试结果表明,经缺氧吸磷驯化后,即使除磷性能欠佳的低浓度电子受体系统污泥也具有良好的反硝化吸磷能力,可见经NO_3~-长期驯化的缺氧吸磷系统有利于筛选以NO_3~-为电子受体的反硝化聚磷菌。     

预缺氧池配水比对Johannesburg工艺脱氮除磷效果的影响

以处理城市污水的中试规模Johannesburg工艺为对象,探讨不同配水比对预缺氧池的反硝化及Johannesburg工艺脱氮除磷效果的影响。在总HRT为12.86 h,预缺氧池HRT为0.6 h的条件下,当配水比分别为0%、10%、20%和30%时,预缺氧池硝酸盐去除率分别为37.67%、78.95%、87.62%和94.95%,对应的厌氧池磷酸盐浓度分别为8.72、19.37、16.1和12.99 mg/L。预缺氧池最佳配水比为10%,此时厌氧段释磷速率、好氧吸磷速率和缺氧吸磷速率分别为6.94、3.17和2.12 mg/(g MLSS·h),厌氧池中磷的最大浓度和污泥中的磷最大含量可达到19.37 mg/L和25.7 mg TP/g MLSS。出水COD、NH3-N、TN和TP等各项水质指标有80%以上的概率达到《城镇污水处理厂污染物排放标准(GB18918-2002)》一级A标准。     

改性方解石的除磷能力研究

选用颗粒方解石,对其表面进行改性,便于磷在其表面的吸附、结晶、沉淀,形成永久性固态磷,加速磷的自然沉淀过程。考察了改性的最佳条件和改性方解石除磷的影响因素。结果表明,方解石的最佳改性条件:改性液TP、Ca2+、HCO-3分别为93.00、120.00、244.00 mg/L,浸泡时间2d;改性方解石具有持续的除磷能力,在实验前76h的平均除磷速率为0.053 0mg/(g·d),而稳定阶段的除磷速率为0.021 4mg/(g·d);待处理水样的Ca2+浓度对改性方解石的除磷效果有较大影响,Ca2+为120.00mg/L时除磷效果最好,碱度对除磷效果的影响很小;pH≤7.30,投加改性方解石系统中磷的去除以改性方解石表面Ca-P结晶为主,而当pH≥8.15时,溶液中发生Ca-P沉淀,而Ca-P结晶逐步减少;水温对改性方解石的除磷效果具有显著影响。     

生物化学协同除磷研究

采用聚合硅酸铝和聚合硅酸铁两种混凝剂,比较了将混凝剂直接投加到反应器中和对生物反应器出水再进行混凝沉淀2种工艺的除磷效果,并对2种混凝剂的除磷效果进行了比较.结果表明:对于聚合硅酸铝,没有生物协同作用;对于聚合硅酸铁,投加量在40 mg/L以下时具有生物协同作用,30 mg/L时协同作用最明显;而且聚合硅酸铁的除磷效果好于聚合硅酸铝.     

生物化学协同除磷研究

采用聚合硅酸铝和聚合硅酸铁两种混凝剂，比较了将混凝剂直接投加到反应器中和对生物反应器出水再进行混凝沉淀2种工艺的除磷效果，并对2种混凝剂的除磷效果进行了比较。结果表明：对于聚合硅酸铝，没有生物协同作用；对于聚合硅酸铁，投加量在40mg／L以下时具有生物协同作用，30mg／L时协同作用最明显；而且聚合硅酸铁的除磷效果好于聚合硅酸铝。     

某城市污水处理厂废水化学除磷沉淀特性及影响因素

通过对西安市某污水处理厂进水、厌氧池上清液、二沉池出水、污泥浓缩水、污泥脱水进行Fe CI_3·6H_2O、PAC除磷实验,并以Fe CI_3·6H_2O为沉淀剂对厌氧池上清液从p H、Fe/P摩尔比、腐殖酸、挥发性脂肪酸(VFA)等因素进行批次实验分析磷去除状况。实验显示,三氯化铁、PAC对进水除磷效果不佳,厌氧池上清液用Fe CI_3·6H_2O为沉淀剂时磷去除率较低,二沉池出水、污泥浓缩水以及污泥脱水用Fe CI_3·6H_2O、PAC时其正磷去除率均可达到80%左右。通过对比不同p H值、Fe/P摩尔比、腐殖酸和VFA浓度对厌氧池上清液除磷效果的影响,结果表明,在p H=4~5,Fe/P=1.3时磷的去除效果达到78%以上,腐殖酸浓度对磷去除率影响不大,VFA在低于10 mg/L和高于60 mg/L时对磷去除率影响较大。     

丝绸厂汰头废水除磷试验研究

针对丝绸厂汰头废水高有机物浓度高氮磷的特点,对该废水的化学除磷工艺及生物化学组合除磷工艺的除磷效能进行了对比研究,考察了有机负荷、运行工况、工艺组合、药剂种类和投加量等对除磷效能的影响.试验结果表明:对汰头废水采用厌氧-生物除磷-生物脱氮-化学除磷组合工艺除磷经济高效,当生物除磷SBBR工艺单元有机负荷为3 kgBOD5/m3·d,运行工况为进水0.5 h-厌氧2 h-曝气4 h-沉淀1 h-排水0.5 h,化学除磷工艺单元投加60 mg/L聚合氯化铝(PAC)时,可使COD及PO3-4分别为10 000 mg/L和114 mg/L的进水,出水COD及PO3-4分别为93 mg/L和0.23 mg/L;总ηCOD91.5%,ηPO3-4为99.8%.其中生物除磷工艺单元承担的ηPO3-4为75%;化学除磷工艺单元承担的ηPO3-4为24.8%.     

Enhanced biological phosphorus removal and recovery

Activated sludge systems designed for enhanced nutrient removal are based on the principle of altering anaerobic and aerobic conditions for growth of microorganisms with a high capacity of phosphorus accumulation. Most often, filamentous bacteria constitute a component of the activated sludge microflora. The filamentous microorganisms are responsible for foam formation and activated sludge bulking. The results obtained confirm unanimously that the filamentous bacteria have the ability of phosphorus uptake and accumulation as polyphosphates. Hydrodynamic disintegration of the foam microorganisms results in the transfer of phosphorus and metal cations and ammonium-nitrogen into the liquid phase. It was demonstrated that the disintegration of foam permits the removal of a portion of the nutrients in the form of struvite.     

污水生物除磷研究进展

水体富营养化是世界性难题,其中磷通常是主要限制因子.生物除磷工艺简单,污泥产量少,可节约能源,运行费用也较低,便于操作和磷的回收.在介绍水体中磷的来源、污染特点及其造成危害的基础上,着重综述了国内外生物除磷的研究进展,并对生物除磷存在的问题和发展趋势提出了一些看法.     

污水生物除磷若干影响因素分析

在系统阐述污水生物除磷机理的基础上,深入分析了微生物群体平衡、城市污水水质、环境因子以及工艺运行参数和运行方式等方面对生物除磷效果的影响.分析结果表明:生物除磷系统的溶解氧浓度不宜太高,一般好氧区DO＜2 mg/L,厌氧区DO＜0.2 mg/L;厌氧段存在硝酸盐对生物释磷有负面影响,缺氧段存在一定浓度的硝酸盐有利于生物聚磷;碳源必须充分、易降解;TKN/COD＜0.1的城市污水有利于生物除磷;pH偏碱性可提高生物除磷效率;低温对生物除磷效果影响不明显.     

Fe^0钝化膜的生物还原及其脱氮除磷

微生物的异化Fe（Ⅲ）还原是一种能够利用Fe（III）作为末端电子受体在无氧条件下氧化有机物的产能过程。结合这一特性，考察了在兼性厌氧／严格厌氧条件下Fe^0钝化膜作为Fe（111）源时的生物还原能力以及对N、P等营养元素的去除效果。结果表明，严格厌氧条件下微生物异化Fe（Ⅲ）还原能力较好，富集培养至7d，累计Fe（II）浓度达到最大，最大产生速率为98．69mg／（L·d），同时TP去除率高达97．1％以上。而体系对NH4-N、TN的去除相对滞后，培养至13d，去除率开始增大，最终分别达到86．6％和76．1％。这为装填有海绵铁＋聚氨酯泡沫载体的SBBR中填料的原位再生问题提供了解决思路。     

The mechanism of enhanced biological phosphorus removal washout and temperature relationships.

In this study, the combined effects of temperature and solids retention time (SRT) on enhanced biological phosphorus removal (EBPR) performance and the mechanism of EBPR washout were investigated. Two pilot-scale University of Cape Town (South Africa) systems fed with synthetic wastewater were operated at 5 and 10 degrees C. The results showed that the phosphorus removal performance was optimum at total SRT ranges of 16 to 24 days and 12 to 17 days for 5 and 10 degrees C, respectively, and steady-state phosphorus removal was greater at the lower temperature. Higher SRT values of up to 32 days at 5 degrees C and 25 days at 10 degrees C slightly reduced EBPR performance as a result of increased extent of endogenous respiration, which consumed internally stored glycogen, leaving less reducing power for poly-hydroxy alkanoate (PHA) formation in anaerobic stages. The phosphorus-accumulating organism (PAO) washout SRTs of the systems were determined as 3.5 days at 5 degrees C and 1.8 days at 10 degrees C, considerably less than the washout SRTs of nitrifiers. Polyphosphorus, the main energy reserve of the EBPR bacterial consortium, was not completely depleted, even at washout points. The inability of EBPR biomass to use glycogen to generate reducing power for PHA formation was the major reason for washout. The results not only suggest that glycogen mechanism is the most rate-limiting step in EBPR systems, but also that it is an integral part of EBPR biochemistry, as proposed originally by Mino et al. (1987), and later others (Pereira et al., 1996, Erdal et al., 2002; Erdal, Z. K., 2002). The aerobic washout SRT values (2.1 and 1.2 days for 5 and 10 degrees C, respectively) of this study did not fit the linear line for PAO washout developed by Mamais and Jenkins (1992). Perhaps this was because the feeds used during this study were chemical-oxygen-demand-limited (acetate-based synthetic feed), whereas the feeds used for their study were phosphorus-limited (external acetate added to domestic wastewater), resulting in different ratios of PAOs and nonPAOs in the biomass.     

强化生物除磷的机理模型研究进展

主要论述了以乙酸盐及葡萄糖作为基质的强化生物除磷的相关机理模型。当以乙酸盐为底物时．重点需要明确导致工艺中微生物代谢模式差异的原因及厌氧条件下还原力供给方式的问题;当以葡萄糖为底物时．主要需要解决厌氧条件下供能方式以及各种微生物之间的关系。某些抑制条件(如供氧不足)可能会促进强化生物除磷效果的实现。强化生物除磷各种机理的差异主要由所驯化的优势微生物种类及其代谢模式不同而造成的。     

Contrast of volatile fatty acid driven and inorganic acid or base driven phosphorus release and uptake in enhanced biological phosphorus removal

Addition of an inorganic acid or base was detrimental to net phosphorus removals in short-term batch experiments, suggesting there might be system upset when pH changes. In contrast, addition of volatile fatty acids (VFAs) increased anaerobic phosphorus release and aerobic phosphorus uptake while maintaining or improving net phosphorus removals. The effect of pH change differed if the acid or base added was inorganic versus organic. Volatile fatty acids that resulted in poly-3-hydroxy-butyrate rather than poly-3-hydroxy-valerate resulted in greater net phosphorus removals, and this corresponded to differences in consumption of reducing equivalents. Acetic acid resulted in improved net phosphorus removal compared to sodium acetate, suggesting that acid forms of VFAs might be superior as supplemental VFAs. It is hypothesized that anaerobic phosphorus release following addition of inorganic acid is primarily a result of phosphorus and proton (H+) symport (excretion from the cell) for pH homeostasis, whereas addition of VFAs results in phosphorus and H+ release to maintain the proton motive force.